A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527066



Internal ID15107673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78172809..78252087hg38UCSC Ensembl
Innerchr11:77883855..77963133hg19UCSC Ensembl
Innerchr11:77561503..77640781hg18UCSC Ensembl
Innerchr11:77561503..77640781hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3879279
hg1979279
hg1879279
hg1779279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703445
Samples
Known GenesGAB2, KCTD21, KCTD21-AS1, USP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527066
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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